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KML001 Enhances Anticancer Activity of Gemcitabine Against Pancreatic Cancer Cells

Authors
Yang, MH[Yang, Moon Hee]Lee, KT[Lee, Kyu Taek]Yang, S[Yang, Sera]Lee, JK[Lee, Jong Kyoon]Lee, KH[Lee, Kwang Hyuck]Rhee, JC[Rhee, Jong Chul]
Issue Date
Jan-2015
Publisher
INT INST ANTICANCER RESEARCH
Citation
ANTICANCER RESEARCH, v.35, no.1, pp.183 - 189
Indexed
SCIE
SCOPUS
Journal Title
ANTICANCER RESEARCH
Volume
35
Number
1
Start Page
183
End Page
189
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/45099
ISSN
0250-7005
Abstract
Background/Aim: Gemcitabine is a drug commonly used to treat pancreatic cancer but chemoresistance to it is a common clinical issue. KML001 (sodium meta-arsenite) has demonstrated certain antitumor activity. The objective of the study was to evaluate the influence of KML001 on the anticancer activity of gemcitabine against pancreatic cancer cells. Materials and Methods: Cell proliferation, migration, and invasion were assessed, as well as the expression of nuclear factor-kappa B (NF-kappa B) p65, epidermal growth factor receptor (EGFR), matrix metalloproteinase-2 (MMP2), and vascular endothelial growth factor-C (VEGFC) in pancreatic cancer cells. Results: Treatment with a combination of KML001 and gemcitabine resulted in significant inhibition of cell proliferation, migration, and invasion, and significantly reduced EGFR and MMP2 expression compared to gemcitabine treatment-alone. Conclusion: Combination treatment of gemcitabine and KML001 could be an effective chemotherapeutic treatment for pancreatic cancer.
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